← Back to catalogue

DermaView II Island Dressing

FDA UDI

Class I (US FDA UDI)

by Dermarite Industries Llc

Identity

Trade Name
DermaView II Island Dressing FDA UDI
Generic Name
Synthetic polymer semi-permeable film dressing, wound-nonadherent FDA UDI
Model / Reference
16240 FDA UDI

Identifiers

Primary DI / UDI-DI
00714196162403 FDA UDI
FDA Product Code
KMK FDA UDI
GMDN Term
Synthetic polymer semi-permeable film dressing, wound-nonadherent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5210 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Synthetic polymer semi-permeable film dressing, wound-nonadherent

DermaView II Island Dressing by Dermarite Industries Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic polymer semi-permeable film dressing, wound-nonadherent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dermarite Industries Llc

Sources (1)

  • FDA UDI cfb927dd-ab3b-4b9b-869a-d34581ba597f 32 fields · synced Jun 1, 2026